Air Pollution and Physical Activity Study (PARC)

April 17, 2026 updated by: Lina Mu, State University of New York at Buffalo

Air Pollution and Physical Activity

This is a small pilot intervention tria lfor exercise and air pollution.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

This is a pilot randomized, control, clinical trial.

We will recruit 24 adults in Buffalo and randomize them to the physical intervention groups. The intervention group will be provided with physical activity courses.

We will follow up all participants until the end of the study.

We will collect their baseline information via questionnaire, and at the end of the follow-up we will collect the exit questionnaire and biospecimen.

The study aims to demonstrate our ability to recruit eligible participants and provide data of the compliance of participants to the intervention.

Study Type

Interventional

Enrollment (Actual)

6

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • New York
      • Buffalo, New York, United States, 14214
        • University at Buffalo

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  • age 35-55 years old
  • plan to stay in Buffalo most of the time in the next three months
  • no adverse conditions

Exclusion Criteria:

• those with unstable or life-threatening medical conditions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Other
  • Allocation: Randomized
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Intervention group 1
This is the physical intervention group 1(n=8).
The intervention group will be provided with training courses for 3 months.
Experimental: Intervention group 2
This is the physical intervention group 2(n=8).
The intervention group will be provided with training courses for 3 months.
No Intervention: Control group
This is the control group (n=8).

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
blood pressure
Time Frame: 3 months
blood pressure will be measured
3 months

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Self-report questionnaire
Time Frame: 3 months
This includes how participants feel about the intervention program
3 months

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Lina Mu, MD,PhD, State University of New York at Buffalo

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

July 25, 2025

Primary Completion (Actual)

February 20, 2026

Study Completion (Actual)

February 25, 2026

Study Registration Dates

First Submitted

April 24, 2024

First Submitted That Met QC Criteria

April 24, 2024

First Posted (Actual)

April 26, 2024

Study Record Updates

Last Update Posted (Actual)

April 22, 2026

Last Update Submitted That Met QC Criteria

April 17, 2026

Last Verified

April 1, 2026

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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